NDC 71335-0522

Metoclopramide Hydrochloride

Metoclopramide Hydrochloride

Metoclopramide Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Metoclopramide Hydrochloride.

Product ID71335-0522_38746352-c02c-4a03-96b3-9b62d8e0176b
NDC71335-0522
Product TypeHuman Prescription Drug
Proprietary NameMetoclopramide Hydrochloride
Generic NameMetoclopramide Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2011-08-22
Marketing CategoryANDA / ANDA
Application NumberANDA071250
Labeler NameBryant Ranch Prepack
Substance NameMETOCLOPRAMIDE HYDROCHLORIDE
Active Ingredient Strength10 mg/1
Pharm ClassesDopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71335-0522-1

30 TABLET in 1 BOTTLE (71335-0522-1)
Marketing Start Date2017-05-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0522-5 [71335052205]

Metoclopramide Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA071250
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-05-01

NDC 71335-0522-3 [71335052203]

Metoclopramide Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA071250
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-05-01

NDC 71335-0522-6 [71335052206]

Metoclopramide Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA071250
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-05-01

NDC 71335-0522-2 [71335052202]

Metoclopramide Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA071250
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-05-01

NDC 71335-0522-4 [71335052204]

Metoclopramide Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA071250
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-05-01

NDC 71335-0522-1 [71335052201]

Metoclopramide Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA071250
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-05-01

Drug Details

Active Ingredients

IngredientStrength
METOCLOPRAMIDE HYDROCHLORIDE10 mg/1

OpenFDA Data

SPL SET ID:fd56674a-841d-4263-91c2-c7d1f2f17a9e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311666
  • 311668

    • Pharmacological Class

    • Dopamine D2 Antagonists [MoA]
    • Dopamine-2 Receptor Antagonist [EPC]

    NDC Crossover Matching brand name "Metoclopramide Hydrochloride" or generic name "Metoclopramide Hydrochloride"

    NDCBrand NameGeneric Name
    0115-1651Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    0115-1652Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    0615-8038Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    0615-8071Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    40032-580METOCLOPRAMIDE hydrochlorideMetoclopramide Hydrochloride
    40032-581METOCLOPRAMIDE hydrochlorideMetoclopramide Hydrochloride
    42254-196Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    42254-266Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    43353-808Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    43386-580METOCLOPRAMIDE hydrochlorideMetoclopramide Hydrochloride
    43386-581METOCLOPRAMIDE hydrochlorideMetoclopramide Hydrochloride
    53808-0623Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    55154-0450Metoclopramide hydrochlorideMetoclopramide hydrochloride
    68071-1996Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    68071-3031Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    68071-3262Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    68071-4551Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    68788-6791Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    68788-9706Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    71335-0528Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    71335-0522Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    55154-5976Metoclopramide hydrochlorideMetoclopramide hydrochloride
    61919-150METOCLOPRAMIDE HYDROCHLORIDEMETOCLOPRAMIDE HYDROCHLORIDE
    63739-293Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    63739-103Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    66689-031Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    67296-0880Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    67296-0883Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    55154-6848Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    55154-8132Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    67296-1810Metoclopramide HydrochlorideMetoclopramide Hydrochloride
    0121-0576Metoclopramidemetoclopramide hydrochloride
    0121-1576Metoclopramidemetoclopramide hydrochloride
    0404-9910MetoclopramideMetoclopramide Hydrochloride
    17856-0537Metoclopramidemetoclopramide hydrochloride
    17856-0576Metoclopramidemetoclopramide hydrochloride
    17856-3727Metoclopramidemetoclopramide hydrochloride
    23155-240MetoclopramideMetoclopramide Hydrochloride
    50436-0576Metoclopramidemetoclopramide hydrochloride
    52584-414MetoclopramideMetoclopramide Hydrochloride
    55154-2353MetoclopramideMETOCLOPRAMIDE HYDROCHLORIDE
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.